Canonical Allele Identifier: CA359953949
Gene: HTR1A HGNC NCBI

Linked Data

dbSNP Id: rs1800044
gnomAD v4: 5-63961061-C-G
MyVariant Identifiers: chr5:g.63256888C>G (hg19) chr5:g.63961061C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63961061C>G , CM000667.2:g.63961061C>G GRCh38
NC_000005.9:g.63256888C>G , CM000667.1:g.63256888C>G GRCh37
NC_000005.8:g.63292644C>G NCBI36
NG_032816.1:g.6232G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000323865.5:c.659G>C MANE Select ENSP00000316244.4:p.Arg220Pro
ENST00000323865.4:c.659G>C ENSP00000316244.3:p.Arg220Pro
NM_000524.3:c.659G>C NP_000515.2:p.Arg220Pro
NM_000524.4:c.659G>C MANE Select NP_000515.2:p.Arg220Pro
Search 100 bp 5'
Search 100 bp 3'